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HOLTER RECORDER & PLAYBACK/ANALYSIS SYS

K822818 Class II Traditional
Decision Date
1982-12-30
Sponsor / Applicant
Marquette Electronics, Inc.

Technical Specification

510(k) Submission ID K822818
Product Code DSH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2800
Decision Date 1982-12-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOLTER RECORDER & PLAYBACK/ANALYSIS SYS received FDA 510(k) clearance under submission number K822818, sponsored by Marquette Electronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1982-12-30.

Classification & Regulation

This clearance is catalogued under FDA product code DSH and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.